2017
DOI: 10.1016/j.polymer.2017.03.020
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Chemistry, polymer dynamics and mechanical properties of a two-part polyurethane elastomer during and after crosslinking. Part I: dry conditions

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Cited by 44 publications
(21 citation statements)
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“…1,[22][23][24][25][26][27][28][29] In this line, Guan et al designed and synthesized a unique uorescent surfactant (TPE-DTAB), which combined both the properties of the aggregation-induced emission (AIE) and amphilicity which together were used to image the macrodispersion of the layered double hydroxide llers (montmorillonite) in the polymer matrix. 30 Wang's group also visualized the entire gelation process of chitosan (CS) by the synthesized AIE uorogenic probe, that is, tetraphenylethene-labelled chitosan (TPE-CS).…”
Section: 21mentioning
confidence: 99%
“…1,[22][23][24][25][26][27][28][29] In this line, Guan et al designed and synthesized a unique uorescent surfactant (TPE-DTAB), which combined both the properties of the aggregation-induced emission (AIE) and amphilicity which together were used to image the macrodispersion of the layered double hydroxide llers (montmorillonite) in the polymer matrix. 30 Wang's group also visualized the entire gelation process of chitosan (CS) by the synthesized AIE uorogenic probe, that is, tetraphenylethene-labelled chitosan (TPE-CS).…”
Section: 21mentioning
confidence: 99%
“…Polyurethane foam has an ageing effect that induced changes in its properties . Especially, as shown in the compression performance assessment for 50 wt%, if a certain amount of HFC‐365mfc is exceeded, performance is dramatically degraded.…”
Section: Resultsmentioning
confidence: 99%
“…Some characteristics polyol bands were assigned in Figure 1(a): the band at 3450 cm -1 indicates the presence of hydroxyl groups; that band at 3008 cm -1 is attributed to the (CH) stretching; 2924 cm -1 to methylene asymmetric stretching ν as (CH 2 ) and 2854 cm -1 to the methylene symmetrical stretching ν ss (CH 2 ) [3,25,26]. The hydroxyl band intensities presented in Figure 2 [3,[26][27][28]. In addition, hydroxyl characteristic bands might also be identified at 1048 cm-1 (primary hydroxyl stretching) and 1096 cm-1 (secondary hydroxyls stretching) [29].…”
Section: Resultsmentioning
confidence: 99%
“…For a quantitative analysis of curing kinetics, isocyanate consumption (% NCO) was calculated using equation (1) [28]: (1) where I Ref is the intensity of the reference band (2924 cm −1 assigned to ν-CH 2 asymmetric stretching), I NCO is the intensity of the isocyanate band (2263 cm -1 ), t cure is the current reaction time, and t 0 is the reaction time of the first measurement spectrum. The isocyanate consumption was plotted as a function of the curing time in Figure 4.…”
Section: Resultsmentioning
confidence: 99%
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